Details: Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio and we are active in over 40 countries across the globe. We continue to steadily grow and are looking to add to our team! Our corporate activities are growing rapidly, and we are currently seeking a full-time, office-based Medical Writer to join our Regulatory Affairs team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. DESCRIPTION OF JOB DUTIES Write clinical study reports, protocols, clinical development plans, FDA briefing documents, and IND, NDA, and MAA modules; Coordinate quality assurance reviews of documents and maintaining audit trails of changes; and Provide input on data analysis planning and interpretation.
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